関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diphosgene | HCID 10426 | — |
| 反応物 | 6-bromo-4-N-(1,3-dimethylpyrazol-4-yl)quinoline-3,4-diamine | HCID 59619708 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 8-bromo-1-(1,3-dimethyl-1H-pyrazol-4-yl)-1,3-dihydro-imidazo[4,5-c]quinolin-2-one | HCID 59619891 | — |
反応手順
To a solution of 6-bromo-N*4*-(1,3-dimethyl-1H-pyrazol-4-yl)-quinoline-3,4-diamine (Stage A.2, 3.15 g, 8.15 mmol) and TEA (1.36 ml, 9.79 mmol) in DCM (65 ml) was added under argon, after cooling with an ice-bath, a solution of trichloromethyl chloroformate (1.08 ml, 8.97 mmol in DCM (65 ml). The mixture was stirred for 25 min at 0° C. Then the RM was quenched with sat. aqueous NaHCO3 (300 ml) and 10 M aqueous NaOH (4 ml) and well stirred. The phases were separated and extracted with EtOAc (3×). The combined organic layers were washed with brine (2×), dried over Na2SO4, filtered and evaporated to dryness to give the title compound as a brownish solid (HPLC tR 2.29 min (Method A); M+H=360; M−H=358 MS-ES)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08476294B2 |
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| 出典データセット | uspto-grants-2013_07 |
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| ORD ID | ord-246aaacf031e4a2598929e88d677f106 |
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| 出典メモ | uspto-grants-2013_07 |
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